Las clasificaciones de pruebas clínicas están diseñadas para ayudar a los médicos a comprender cómo los cambios genéticos, conocidos como variantes, podrían afectar la salud de una persona y guiar las decisiones médicas. Las variantes se etiquetan como Causantes de Enfermedad (dañinas), Probablemente Causantes de Enfermedad, Efecto Desconocido (impacto desconocido), Probablemente Sin Efecto (probablemente no dañinas) y Sin Efecto (no dañinas). Esta clasificación se basa en una combinación de antecedentes familiares, pruebas de laboratorio y predicciones por computadora para determinar el impacto de las variantes.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
T
T
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/T has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
A
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
A
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters A/A is thought to have no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.
Genotype
A
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters A/G has an unknown effect on your disease risk. This means that the scientific evidence is still somewhat unclear about its effect.